T-relief Extra Strength Tablet, Chewable
NDC Package 62795-1041-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

T-relief Extra Strength (arnica montana, calendula officinalis flowering, hamamelis virginiana root bark/stem, baptisia tinctoria root, bellis perennis, echinacea, unspecified, aconitum napellus, matricaria chamomilla, achillea millefolium, atropa belladonna, hypericum perforatum, ruta graveolens flowering top and comfrey root) tablets is relieves muscle, Joint, back, nerve and arthritis pain. This formulation utilizes a tablet, chewable delivery system. Marketed by Medinatura Inc, this product is identified by NDC 62795-1041.

Identification & Billing

NDC Package Code
62795-1041-2
Package Description
1 BOTTLE in 1 CARTON / 90 TABLET, CHEWABLE in 1 BOTTLE
Product Code
62795-1041
11-Digit Billing Format
62795104102
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA

Clinical Specifications

Proprietary Name
T-relief Extra Strength
Non-Proprietary Name
Arnica Montana, Calendula Officinalis Flowering, Hamamelis Virginiana Root Bark/stem, Baptisia Tinctoria Root, Bellis Perennis, Echinacea, Unspecified, Aconitum Napellus, Matricaria Chamomilla, Achillea Millefolium, Atropa Belladonna, Hypericum Perforatum, Ruta Graveolens Flowering Top And Comfrey Root
Substance Name
Achillea Millefolium; Aconitum Napellus; Arnica Montana; Atropa Belladonna; Baptisia Tinctoria Root; Bellis Perennis; Calendula Officinalis Flowering Top; Comfrey Root; Echinacea, Unspecified; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum; Matricaria Chamomilla; Ruta Graveolens Flowering Top
Dosage Form
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Relieves muscle, Joint, back, nerve and arthritis pain.

Regulatory & Marketing

Labeler Name
Medinatura Inc
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
02-01-2018
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (62795-1041). Click a package code to view its specific billing and regulatory data.

62795-1041-3
4 TABLET, CHEWABLE in 1 POUCH
62795-1041-4
1 BOTTLE in 1 CARTON / 100 TABLET, CHEWABLE in 1 BOTTLE
62795-1041-5
250 TABLET, CHEWABLE in 1 BOTTLE
62795-1041-6
100 TABLET, CHEWABLE in 1 BOTTLE
62795-1041-7
60 TABLET, CHEWABLE in 1 BOTTLE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 62795-1041-2 identifies a specific commercial package of 1 bottle in 1 carton / 90 tablet, chewable in 1 bottle of T-relief Extra Strength, a human over the counter drug labeled by Medinatura Inc. This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package. This tablet, chewable is formulated for oral use and contains achillea millefolium; aconitum napellus; arnica montana; atropa belladonna; baptisia tinctoria root; bellis perennis; calendula officinalis flowering top; comfrey root; echinacea, unspecified; hamamelis virginiana root bark/stem bark; hypericum perforatum; matricaria chamomilla; ruta graveolens flowering top as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Medinatura Inc on February 01, 2018. The current certification is valid through December 31, 2026.

How is this Medinatura Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62795104102. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
62795-1041-2
11-Digit CMS (5-4-2)
62795-1041-02

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.